The androgen receptor transcriptional program in castration-resistant prostate cancer: Cell lines vs. tissue samples

Jeffrey E. Roth, Cody J. Peer, Douglas K. Price, William D. Figg*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

The androgen receptor (AR) is central to the initiation and progression of prostate cancer, even after castration. Its transcriptional activity has previously been studied in cell lines. A group at the University of Cambridge recently outlined the AR transcriptional program in tissue samples, with an emphasis on castration-resistant tumors. AR binding sites, gene-expression changes (in xenografts), and potential transcription factor interactions were notably different from those observed in cultured cells. These discrepancies suggest a distinct signaling network for the AR in vivo and serve as a reminder that results from in vitro models should be checked against clinical realities.

Original languageEnglish
Pages (from-to)16-18
Number of pages3
JournalCancer Biology and Therapy
Volume15
Issue number1
DOIs
StatePublished - Jan 2014
Externally publishedYes

Keywords

  • Androgen receptor
  • Binding site
  • Castrationresistant prostate cancer
  • Transcription factor
  • Transcriptional program

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